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Multizen Industry (Shenzhen) Ltd.

⚠️ Moderate Risk

FEI: 3004323847 • Shenzhen, Yandong • CHINA

FEI

FEI Number

3004323847

📍

Location

Shenzhen, Yandong

🇨🇳

Country

CHINA
🏢

Address

Blk 31, Long Wang Shrine Ind. Est F/4, Bai Shi Xia; Fu Yong Town, Shenzhen, Yandong, China

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
1
Unique Violations
11/25/2008
Latest Refusal
11/25/2008
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

2492×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
11/25/2008
33MGT01GEL CUPS, FRUIT FLAVORED
249FILTHY
New York District Office (NYK-DO)
11/25/2008
33MGT01GEL CUPS, FRUIT FLAVORED
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is Multizen Industry (Shenzhen) Ltd.'s FDA import refusal history?

Multizen Industry (Shenzhen) Ltd. (FEI: 3004323847) has 2 FDA import refusal record(s) in our database, spanning from 11/25/2008 to 11/25/2008.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Multizen Industry (Shenzhen) Ltd.'s FEI number is 3004323847.

What types of violations has Multizen Industry (Shenzhen) Ltd. received?

Multizen Industry (Shenzhen) Ltd. has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Multizen Industry (Shenzhen) Ltd. come from?

All FDA import refusal data for Multizen Industry (Shenzhen) Ltd. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.